@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_head {
   this: np:hasAssertion dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_assertion ;
    np:hasProvenance dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_provenance ;
    np:hasPublicationInfo dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_assertion a np:Assertion .
  dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_provenance a np:Provenance .
  dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_assertion {
   miriam-gene:348 a ncit:C16612 .
  lld:C0002395 a ncit:C7057 .
  dgn-gda:DGNde0d89f47530e9947aca071bf4ca4f0c sio:SIO_000628 miriam-gene:348 , lld:C0002395 ;
    a sio:SIO_001121 .
}
dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_provenance {
   dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_assertion dcterms:description "[When statistical analysis was conducted after the exclusion of the APOE epsilon2 allele, the frequency of the APOE epsilon4 allele in AD patients was significantly higher than that in controls (P &lt; 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:11285089 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP313074.RAfpYzGVEkjlc7qHnDFn0TzHUJu6i527uRgQ85haWldPA130_publicationInfo {
   this: dcterms:created "2016-05-13T12:44:07+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}